Syndrome DB - Table Of Contents encephalocraniofacial angiomatosis. encephalofacial angiomatosis. encephalofacial neuroangiomatosis. encephalotrigeminal http://www.nlm.nih.gov/mesh/jablonski/syndrome_toc/toc_e.html
E Index Please click on the "box below" to view the following topics. Please click on the "box below" to view the following topics. EMOTIONS, FEARS. encephalofacial angiomatosis. ENCEPHALOMYELOPATHY. ENCEPHALOTRIGEMINAL ANGIOMATOSIS http://www.childhealthinfo.com/eindex.htm
Extractions: A B C D ... Z Please click on the "box below" to view the following topics. E Part I EAR ANOMALIES/DISORDERS EAR INFECTIONS, ETC. ... ENCHONDROMATOSIS Please click on the "box below" to view the following topics. E Part II ENDOCRINE DISEASES ENTERAL NUTRITION ... MoreInfo@ChildHealthInfo.com
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BizLand Angiomatosis. This image depicts the leptomeningeal angiomatosis characteristicof encephalofacial angiomatosis (SturgeWeber Disease). http://www.braincampus.com/neupath/tumor/angiomat.html
Brain Tumor Brain Tumor Angiomatosis This image depicts the leptomeningeal angiomatosischaracteristic of encephalofacial angiomatosis (SturgeWeber Disease). http://nanonline.org/nandistance/mtbi/NeuroIll/tumor/angio.html
Extractions: Angiomatosis This image depicts the leptomeningeal angiomatosis characteristic of encephalofacial angiomatosis (Sturge-Weber Disease). Note the mild atrophy of the affected hemisphere. Angiomatosis (Encephalofacial; Sturge-Weber Disease): This is a developmental disorder that involves a capillary-venous angioma of the face and leptomeninges of the brain. The facial angioma is also called a nevus flammeus or "port wine stain". Most lesions are unilateral. Although the angioma is present at birth, the neurological manifestations of the disorder emerge over the course of development. They may include focal seizures, contralateral spastic hemiplegia, hemisensory loss and visual field defects. There may be cortical atrophy and calcifications.
Extractions: Syndrome Sturge-Weber syndrome (SWS) Synonyms Dimitri disease Jahnke syndrome Kalischer syndrome Lawford syndrome Müller syndrome Parkes Weber syndrome Parkes Weber and Dimitri syndrome Schirmer syndrome Sturge disease Sturge syndrome Sturge-Kalischer-Weber syndrome Sturge-Weber angiomatosis Sturge-Weber anomalad Sturge-Weber-Dimitri syndrome Sturge-Weber-Krabbe syndrome Sturge-Weber-Thoma syndrome Weber syndrome Weber-Dimitri syndrome angioma capillare et venosum calcificans angiomatosis encephalofacialis angiomatosis meningoulofacialis angiomatosis-oculo-orbito-thalamo-encephalic syndrome cerebrocutaneous angiomatosis cutaneocerebral angioma ectoneurodermal hamartoma encephalocraniofacial angiomatosis encephalofacial angiomatosis encephalofacial neuroangiomatosis encephalotrigeminal angiomatosis encephalotrigeminal syndrome fourth phacomatosis meningeal capillary angiomatosis meningofacial angiomatosis meningo-oculofacial angiomatosis neuroangiomatosis encephalofacialis neurocutaneous syndrome neuroectodermal hamartoma neuro-oculocutaneous angiomatosis neuroretinoangiomatosis nevoid amentia trigemino-encephalo-angiomatosis Summary A group of neurocutaneous disorders manifested by facial and leptomeningeal angiomas, ipsilateral gyriform calcifications of the cerebral cortex, seizures, development delay, hemiplegia, emotional and behavioral problems, and glaucoma and other ocular disorders. Nevus flammeus on the side of the face ipsilateral to angiomatosis sometimes extends to neck, chest, and back. Angiomatosis may occasionally involve the choroid plexus, thyroid, pituitary gland, lungs, gastrointestinal organs, pancreas, ovaries, and thymus. Correlation between the distribution of the nevus and the course of the trigeminal nerve is responsible for naming the syndrome "trigemino-encephalo-angiomatosis," but later findings found the relationship to be fortuitous. The syndrome frequently occurs in incomplete forms, presenting different combinations of symptoms.
NORD - National Organization For Rare Disorders, Inc. Sturge Weber Syndrome Dimitri Disease; encephalofacial angiomatosis;Encephalotrigeminal Angiomatosis; Leptomeningeal Angiomatosis; http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Sturge Weber
Definitions Of Genetic Disorders-E. htm. encephalofacial angiomatosis (SturgeWeber) http//www.ninds.nih.gov/health_and_medical/disorders/sturge_doc.htm.Encephalomyelopathy http://www.icomm.ca/geneinfo/def-e.htm
IComm: File Not Found! Hydrocephalus Parents Support Group http//www.stepstn.com/nord/org_sum/933.htm.encephalofacial angiomatosis.. (SturgeWeber). Sturge http://www.icomm.ca/geneinfo/e.htm
Extractions: Back to Home Web Review of Ophthalmology AKAs Age-Related Macular Degeneration (AMD) Age-related maculopathy Senile macular degeneration Dystrophy any disorder arising from defective or faulty nutrition Granular corneal dystrophy stroma clear? Groenouws type I Macular corneal dystrophy indistinct irregular borders, intervening cloudy stroma Groenouws type II Lattice corneal dystrophy Biber-Haab-Dimmer dystrophy Epithelial dystrophy MDF dystrophy; map-dot-fingerprint dystrophy Cogans microcystic dystrophy ABMD; anterior basment membrane dystrophy Grave's Eye Disease Thyroid ophthalmopathy Thyroid orbitopathy Thyroid-related immune orbitopathy (TRIO) Von Basedow eye disease (in European literature) Large cell lymphoma Histiocytic lymphoma (old literature) Reticulum cell sarcoma (old literature) Phacoantigenic endophthalmitis
WebMD - nord Encephalitis, Japanese nord Encephalitis, Rasmussen's nord Encephalocelenord encephalofacial angiomatosis nord Encephalomyelitis, Myalgic nord http://my.webmd.com/content/healthwise/118/29495.htm
Searchalot Directory For E 4); Emetophobia (6); Emphysema (103); Empty Sella Syndrome (6); Encephalitis(8); encephalofacial angiomatosis (4); Encephalomyelitis http://www.searchalot.com/Top/Health/ConditionsandDiseases/E/
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